These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

203 related articles for article (PubMed ID: 32901963)

  • 1. The evolution of the nosology of osteogenesis imperfecta.
    Chetty M; Roomaney IA; Beighton P
    Clin Genet; 2021 Jan; 99(1):42-52. PubMed ID: 32901963
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Osteogenesis imperfecta: clinical diagnosis, nomenclature and severity assessment.
    Van Dijk FS; Sillence DO
    Am J Med Genet A; 2014 Jun; 164A(6):1470-81. PubMed ID: 24715559
    [TBL] [Abstract][Full Text] [Related]  

  • 3. What is new in genetics and osteogenesis imperfecta classification?
    Valadares ER; Carneiro TB; Santos PM; Oliveira AC; Zabel B
    J Pediatr (Rio J); 2014; 90(6):536-41. PubMed ID: 25046257
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Ultrastructural and histological findings on examination of skin in osteogenesis imperfecta: a novel study.
    Balasubramanian M; Wagner BE; Peres LC; Sobey GJ; Parker MJ; Dalton A; Arundel P; Bishop NJ
    Clin Dysmorphol; 2015 Apr; 24(2):45-54. PubMed ID: 25436829
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Genotypes and phenotypes of nine Uygur children with osteogenesis imperfecta in Xinjiang].
    Luo YF; Dilihuma J; Sun GH; Reyilanmu B; Liang L; Du XY; Mireguli M
    Zhonghua Er Ke Za Zhi; 2020 Feb; 58(2):135-139. PubMed ID: 32102151
    [No Abstract]   [Full Text] [Related]  

  • 6. A Dyadic Nosology for Osteogenesis Imperfecta and Bone Fragility Syndromes 2024.
    Sillence DO
    Calcif Tissue Int; 2024 Jun; ():. PubMed ID: 38942908
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Genetic epidemiology, prevalence, and genotype-phenotype correlations in the Swedish population with osteogenesis imperfecta.
    Lindahl K; Åström E; Rubin CJ; Grigelioniene G; Malmgren B; Ljunggren Ö; Kindmark A
    Eur J Hum Genet; 2015 Aug; 23(8):1042-50. PubMed ID: 25944380
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Osteogenesis imperfecta: an expanding panorama of variants.
    Sillence D
    Clin Orthop Relat Res; 1981 Sep; (159):11-25. PubMed ID: 7285446
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Skeletal phenotypes in adult patients with osteogenesis imperfecta-correlations with COL1A1/COL1A2 genotype and collagen structure.
    Hald JD; Folkestad L; Harsløf T; Lund AM; Duno M; Jensen JB; Neghabat S; Brixen K; Langdahl B
    Osteoporos Int; 2016 Nov; 27(11):3331-3341. PubMed ID: 27256333
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Impact of Intrinsic Muscle Weakness on Muscle-Bone Crosstalk in Osteogenesis Imperfecta.
    Gremminger VL; Phillips CL
    Int J Mol Sci; 2021 May; 22(9):. PubMed ID: 34066978
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Type V osteogenesis imperfecta: a new form of brittle bone disease.
    Glorieux FH; Rauch F; Plotkin H; Ward L; Travers R; Roughley P; Lalic L; Glorieux DF; Fassier F; Bishop NJ
    J Bone Miner Res; 2000 Sep; 15(9):1650-8. PubMed ID: 10976985
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Comprehensive genetic analyses using targeted next-generation sequencing and genotype-phenotype correlations in 53 Japanese patients with osteogenesis imperfecta.
    Ohata Y; Takeyari S; Nakano Y; Kitaoka T; Nakayama H; Bizaoui V; Yamamoto K; Miyata K; Yamamoto K; Fujiwara M; Kubota T; Michigami T; Yamamoto K; Yamamoto T; Namba N; Ebina K; Yoshikawa H; Ozono K
    Osteoporos Int; 2019 Nov; 30(11):2333-2342. PubMed ID: 31363794
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Letter to the editor: Re: Pathogenic mechanisms of osteogenesis imperfecta, evidence for classification.
    Dalgleish R; Micha D; Superti-Furga A; van Dijk FS; Sillence DO
    Orphanet J Rare Dis; 2024 Jul; 19(1):272. PubMed ID: 39030555
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Osteogenesis imperfecta type VI: a form of brittle bone disease with a mineralization defect.
    Glorieux FH; Ward LM; Rauch F; Lalic L; Roughley PJ; Travers R
    J Bone Miner Res; 2002 Jan; 17(1):30-8. PubMed ID: 11771667
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Dental findings in osteogenesis imperfecta: I. Occurrence and expression of type I dentinogenesis imperfecta.
    Lukinmaa PL; Ranta H; Ranta K; Kaitila I
    J Craniofac Genet Dev Biol; 1987; 7(2):115-25. PubMed ID: 3624417
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Scoliosis in osteogenesis imperfecta caused by COL1A1/COL1A2 mutations - genotype-phenotype correlations and effect of bisphosphonate treatment.
    Sato A; Ouellet J; Muneta T; Glorieux FH; Rauch F
    Bone; 2016 May; 86():53-7. PubMed ID: 26927310
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Osteogenesis imperfecta type III. Delineation of the phenotype with reference to genetic heterogeneity.
    Sillence DO; Barlow KK; Cole WG; Dietrich S; Garber AP; Rimoin DL
    Am J Med Genet; 1986 Mar; 23(3):821-32. PubMed ID: 3953678
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Genotype-phenotype relationship in a large cohort of osteogenesis imperfecta patients with COL1A1 mutations revealed by a new scoring system.
    Li LJ; Lyu F; Song YW; Wang O; Jiang Y; Xia WB; Xing XP; Li M
    Chin Med J (Engl); 2019 Jan; 132(2):145-153. PubMed ID: 30614853
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Osteogenesis imperfecta at the beginning of bone and joint decade.
    Primorac D; Rowe DW; Mottes M; Barisić I; Anticević D; Mirandola S; Gomez Lira M; Kalajzić I; Kusec V; Glorieux FH
    Croat Med J; 2001 Aug; 42(4):393-415. PubMed ID: 11471191
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Osteogenesis imperfecta types I-XI: implications for the neonatal nurse.
    Womack J
    Adv Neonatal Care; 2014 Oct; 14(5):309-15; quiz 316-7. PubMed ID: 24950034
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.